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1.
Polyclithrum ponticum sp. n. is described and P. mugilini Rogers, 1967 is redescribed. Both monogenean species are parasites of Mugil cephalus in the Black Sea. The new species differs from P. mugilini, P. alberti and P. boegeri by the lesser size of anchors, while it is distinguished from P. corallense by the larger size of these structures. P. ponticum sp. n. differs from all formerly described species by the greater length of dorsal connective bar. In both species from the Black Sea, "ear-like" structures situated near the external roots of anchors are described for the first time. It is suggested, that these structures take part in longitudinal, two-lobe folding of the haptor. The process of opening the haptor is probably performed by the additional bars of the haptor (bars 2 and 3 after: Rogers, 1967), joined to each other and with the anchors. The fifth pair of additional bars (Ernst e. a., 2000) derives from the "beard" of ventral connective bar and is united with its basal part. The sixth pair of additional bars (Ernst e. a., 2000) is considered as a typical "ribs" of the haptor, and therefore the "ribs" are represented by three pairs. Differences between marginal hooks of P. ponticum sp. n. and P. mugilini are insignificant, that probably depends on the presence of "ribs" of the haptor. Based on the subdivision of marginal hooks into two groups, the presence of additional supporting structure in the haptor, and the presence of the seminal receptacle, it is suggested that the subfamily Polyclithrinae Rogers, 1967 should include the genera Polyclithrum Rogers, 1967, Swingleus Rogers, 1969, Macrogyrodactylus Mamlberg, 1959, and probably Fundulotrema Hargis, 1955. Based on such characters as the lack of the anchors, the presence of suckers in the haptor, and ovipositing of eggs, it seems to be expedient to use the following taxa in systematics of gyrodactylids: Isancistrinae Fuhrmann, 1928 (genera Isancistrum, Anacanthocotyle); Gyrdicotylinae Vercammen-Grandjean, 1960 (Gyrdicotyle) and Ooegyrodactylinae Harris, 1983 (genera Phanerothecium, Ooegyrodactylus, Nothogyrodactylus, Hyperopletes).  相似文献   

2.
Data on the ontogeny of the posterior haptor of monogeneans were obtained from more than 150 publications and summarised. These data were plotted into diagrams showing evolutionary capacity levels based on the theory of a progressive evolution of marginal hooks, anchors and other attachment components of the posterior haptor in the Monogenea (Malmberg, 1986). 5 + 5 unhinged marginal hooks are assumed to be the most primitive monogenean haptoral condition. Thus the diagrams were founded on a 5 + 5 unhinged marginal hook evolutionary capacity level, and the evolutionary capacity levels of anchors and other haptoral attachement components were arranged according to haptoral ontogenetical sequences. In the final plotting diagram data on hosts, type of spermatozoa, oncomiracidial ciliation, sensilla pattern and protonephridial systems were also included. In this way a number of correlations were revealed. Thus, for example, the number of 5 + 5 marginal hooks correlates with the most primitive monogenean type of spermatozoon and with few sensillae, many ciliated cells and a simple protonephridial system in the oncomiracidium. On the basis of the reviewed data it is concluded that the ancient monogeneans with 5 + 5 unhinged marginal hooks were divided into two main lines, one retaining unhinged marginal hooks and the other evolving hinged marginal hooks. Both main lines have recent representatives at different marginal hook evolutionary capacity levels, i.e. monogeneans retaining a haptor with only marginal hooks. For the main line with hinged marginal hooks the name Articulon-choinea n. subclass is proposed. Members with 8 + 8 hinged marginal hooks only are here called Proanchorea n. superord. Monogeneans with unhinged marginal hooks only are here called Ananchorea n. superord. and three new families are erected for its recent members: Anonchohapteridae n. fam., Acolpentronidae n. fam. and Anacanthoridae n. fam. (with 7 + 7, 8 + 8 and 9 + 9 unhinged marginal hooks, respectively). Except for the families of Articulonchoinea (e.g. Acanthocotylidae, Gyrodactylidae, Tetraonchoididae) Bychowsky's (1957) division of the Monogenea into the Oligonchoinea and Polyonchoinea fits the proposed scheme, i.e. monogeneans with unhinged marginal hooks form one old group, the Oligonchoinea, which have 5 + 5 unhinged marginal hooks, and the other group form the Polyonchoinea, which (with the exception of the Hexabothriidae) has a greater number (7 + 7, 8 + 8 or 9 + 9) of unhinged marginal hooks. It is proposed that both these names, Oligonchoinea (sensu mihi) and Polyonchoinea (sensu mihi), will be retained on one side and Articulonchoinea placed on the other side, which reflects the early monogenean evolution. Except for the members of Ananchorea [Polyonchoinea], all members of the Oligonchoinea and Polyonchoinea have anchors, which imply that they are further evolved, i.e. have passed the 5 + 5 marginal hook evolutionary capacity level (Malmberg, 1986). There are two main types of anchors in the Monogenea: haptoral anchors, with anlages appearing in the haptor, and peduncular anchors, with anlages in the peduncle. There are two types of haptoral anchors: peripheral haptoral anchors, ontogenetically the oldest, and central haptoral anchors. Peduncular anchors, in turn, are ontogenetically younger than peripheral haptoral anchors. There may be two pairs of peduncular anchors: medial peduncular anchors, ontogentically the oldest, and lateral peduncular anchors. Only peduncular (not haptoral) anchors have anchor bars. Monogeneans with haptoral anchors are here called Mediohaptanchorea n. superord. and Laterohaptanchorea n. superord. or haptanchoreans. All oligonchoineans and the oldest polyonchoineans are haptanchoreans. Certain members of Calceostomatidae [Polyonchoinea] are the only monogeneans with both (peripheral) haptoral and peduncular anchors (one pair). These monogeneans are here called Mixanchorea n. superord. Polyonchoineans with peduncular anchors and unhinged marginal hooks are here called the Pedunculanchorea n. superord. The most primitive pedunculanchoreans have only one pair of peduncular anchors with an anchor bar, while the most advanced have both medial and lateral peduncular anchors; each pair having an anchor bar. Certain families of the Articulonchoinea, the Anchorea n. superord., also have peduncular anchors (parallel evolution): only one family, the Sundanonchidae n. fam., has both medial and lateral peduncular anchors, each anchor pair with an anchor bar. Evolutionary lines from different monogenean evolutionary capacity levels are discussed and a new system of classification for the Monogenea is proposed.In agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. EditorIn agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. Editor  相似文献   

3.
Gyrodactylus moldovicus sp. n. found on gills, body and in nasal cavities of the European mudminnow (Umbra krameri) differs from G. slovacicus Ergens, 1963 also living on the this host by bigger size of the body, anchors and marginal hooks; from G. cylindriformes Mueller et Van Cleave, 1932 living on the American mudminnow Umbra limi--by bigger size of the body; from G. limi Wood et Mizelle, 1957 also from U. limi--by the form of ventral and dorsal bars and form of marginal hooks. It differs from other freshwater gyrodactylids by special type of marginal hooks which have a hook-like end of the blade. Gyrodactylus moldovicus, G. slovacicus and G. limi have marginal hooks of quite different morphological types. By the morphology of anchors, ventral and sometimes dorsal bars and also morphology of cirrus, G. moldovicus is most related to three species from Cyprininae: G. stankovichi Ergens, 1970, G. longoacuminatus Zitnan, 1964 f. typica and G. shulmani Ling, 1962.  相似文献   

4.
Gerasev PI 《Parazitologiia》2002,36(2):146-157
It is considered that in Anacanthorinae, Markewitschiana and Pseudacolpenteron pavlovskii (Dactylogyridae s. s.) the anchors are absent originally. In the other dactylogyrids (s. l.) without anchors (Pseudacolpenteron ignotus; Acolpenteron; Anonchohaptor-Icelanchohaptor; Kritskyia-Telethecium-Pavanelliela) these structures are lost. In related genera Rhinoxenus and Nanotrema the dorsal pair of anchors is transformed into the "spikes"; in Heteronchocleidinae there is one anchor; in Trinigyrus and Schilbetrematoides are two anchors; and in Urogyrus three anchors are reduced. But in Rhinonaster, Cacatyocotyle, Callceostomella, Neocalseostoma elongatum and Pseudodactylogyridae the presence of one pair of ventral "peduncular" or "haptoral" anchors appear to be the original state. For Anacanthorinae and Dactylogyridae s. s. the presence of 18-16 hooks, original lacking of anchors, appearance of one pair of them, evolutionary development and subsequent reduction of these structures are characteristic. In the dactylogyrids (s. l.) having two pairs of anchors and 14 hooks, one pair of the anchors is present originally, then usually the second dorsal pair grows up, and finally, the reduction of a part of anchors or all the anchors is possible. In the 16-hooked dactylogyrids (s. l.) having two pairs of anchors (Tetraonchinea, Amphibdellainea, Neodactylodiscinea) the original lacking or reduction of the anchors is not reported. The author considers, that it is unwarranted to unite all dactylogyrids (s. l.) without anchors into the superorder Ananchorea Malmberg, 1990 or to postulate the original presence of the two pairs of ventral anchors in this group. It is also impossible to unit all dactylogyrids (s. l.) having 0-4 anchors and 18-14 hooks into Dactylogyridae sensu Boeger et Kritsky, 1993.  相似文献   

5.
Cornutohaptor nigrescensi n. sp. (Diplectanidae) is described from the gills of the black snook, Centropomus nigrescens (Perciformes: Centropomidae) from the Pacific coast of Mexico. Cornutohaptor n. gen. is proposed for this new species and is characterized by possessing 2 intestinal ceca terminating blindly; a germarium looping right intestinal cecum; bilobed testis; 2 seminal vesicles; 7 pairs of hooks, each with protruding thumb; a grooved ventral bar and coiled male copulatory organ (MCO); an accessory piece comprising a "baglike structure" with an appendage; dorsal bars associated parallelly to body midline; and no adhesive accessory organs on the haptor. Cornutohaptor differs from all confamilial genera by including species with anchors with straight and deep root longest, hook pair 1 reduced in size, MCO with counterclockwise rings, and by the morphology of the accessory piece. Cornutohaptor nigrescensi most closely resembles species of Murraytrema Price, 1937, Lobotrema Tripathi, 1937, and Murraytrematoides Yamaguti, 1958, because of the absence of squamodiscs or lamellodiscs on the haptor and tegumental scales on the posterior portion of the body. Cornutohaptor differs from these genera in the position and number of haptoral bars (2 bars in Lobotrema spp., dorsal bars transversally associated in Murraytrema and Murraytrematoides spp.) and in having a coiled MCO (copulatory organ is a comparatively straight, poorly sclerotized tube in Murraytrematoides spp.). This is the first diplectanid described from a centropomid along the Pacific coast of Mexico.  相似文献   

6.
The monotypic Philureter n. gen. (Ancyrocephalinae; Dactylogyridae) is proposed to accommodate Philureter trigoniopsis n. sp. with the following features: presence of a cuplike ventral haptor armed with 14 hooks and 2 anchor/bar complexes; dorsal pair of anchors poorly defined and variable in shape, 1 frequently absent; tandem, intercecal gonads, testis bilaterally lobulated. Philureter trigoniopsis n. sp. is described from the ureters and urinary bladder of Galaxias maculatus (Jenyns, 1842) (Osmeriformes) in Patagonian Andean lakes, Argentina.  相似文献   

7.
A new species of Kritskyia inhabits the urinary bladder of the "curimba", Prochilodus lineatus in the floodplain of the high Paraná river. The new species resembles others members of Kritskyia in the following features: haptor lacking anchors and with 14 hooks marginal, posterior male copulatory organ non articulated with the accessory piece and vagina a sclerotized tube. However, it differs from the known species mainly by the shape of the copulatory complex. This is the third endoparasitic monogenean species reported from freshwater Neotropical fish.  相似文献   

8.
Calicobenedenia polyprioni n. sp. (Capsalidae) is described from the external surfaces (skin and eye) of wreckfish, Polyprion americanus (Teleostei, Perciformes, Polyprionidae), from the north Atlantic Ocean. The monotypic Calicobenedenia n. gen. is proposed for this species and is characterized, in part, by its members possessing an aseptate haptor armed with 14 submarginal hooks and 1 pair of anchors, a common genital pore opening marginally immediately posterior to the left cephalic lobe, 2 testes juxtaposed near the body midlength, and by lacking cephalic suckers or adhesive discs, accessory haptoral sclerites, and a uterine valve. The new genus most closely resembles Entobdella, which differs from Calicobenedenia by having an aseptate haptor armed with 14 submarginal hooks, 2 pairs of anchors, and a pair of accessary sclerites.  相似文献   

9.
Three new species of Ancistrohaptor n. g. are described from the gills of three species of Triportheus (Characidae) collected from the environs of Manaus, Amazonas, Brazil: A. falcatum n. sp. from T. elongatus; and A. falciferum n. sp. and A. falcunculum n. sp. from T. angulatus, T. albus and T. elongatus. Ancistrohaptor n. g. is proposed for species possessing overlapping gonads, a dextral or dextroventral vaginal aperture, a coiled (counter-clockwise) male copulatory organ, two accessory pieces in the copulatory complex, and a haptor armed with two pairs of anchors (ventral anchor with elongate shaft), dorsal and ventral bars and 14 hooks; hook pair 1 (ventral) anterior to ventral bar, pairs 2–4 (ventral) lying bilaterally anterior to ventral anchor bases, pair 5 (ventral) associated with distal end of ventral anchor shafts, and pairs 6 and 7 (dorsal) bilateral about midway along haptoral length. Parasite-host and host-parasite lists of the Ancyrocephalinae from neotropical Characiformes are provided.  相似文献   

10.
The hypothesis of the origin and evolution of the hamuli in monogeneans is proposed. It is suggested that the hamuli originated as the adult attachment organs of protomonogeneans inhabited the gills of the first vertebrates. Primarily they were represented by two lateral pairs of large hooks disposed anterior to the larval haptor. The fundamental direction in the evolution of monogeneans was the concentration of all attachment structures on the growing haptor. It the course of this evolutionary process, the hamuli onchoblasts migrated to the haptor, in which they had reached the position in the hind part of the haptor. The neotenic evolution of the Dactylogyridea and Gyrodactyloidea resulted in the forming new hamuli pairs. The hooks of opposite sides of the haptor are joined in a single complex within each side by the transverse plates (bars). So the presence of 4 hamuli is plesiomorphy for all the monogeneans and the presence of the transverse bars and new hamuli pairs are apomorphy for the Dactylogyridea and Gyrodactyloidea, whose evolution was linked with that of the Teleostei. The origin of the new hamuli pairs and transverse bars in the Dactylogyridea and Gyrodactyloidea appears to be a convergence.  相似文献   

11.
Gyrodactylus gvozdevi n. sp. (Gyrodactylidae: Monogenea) is described from the skin of the freshwater fish Noemacheilus dorsalis (Kessler) (Cobitidae: Cypriniformes) from Kazakhstan. This species is most closely related to G. pseudonemachili Ergens & Bykhovsky, 1967 in the shape and size of the anchors and both the ventral and dorsal bars, but can be distinguished from it by the shape and size of the hookproper of the marginal hooks.  相似文献   

12.
Seasonal variations in the size and shape of the marginal hooks, anchors and ventral bar of the opisthaptor of Gyrodactylus derjavini Mikailov, 1975 were studied. The G. derjavini specimens were collected from brown trout Salmo trutta L. parr and Atlantic salmon S. salar L. parr in the River Sandvikselva, southeastern Norway. Samples were taken at roughly monthly intervals during a 13-month period. The marginal hooks, anchors and ventral bars showed considerable seasonal variation in size, but varied very little in shape. The size increased when the water temperature decreased and vice versa.  相似文献   

13.
Ultrastructural studies were carried out on the surface of Vallisia indica, found on the gills of Scomberoides commersonianus in the Indian ocean. Tegumental serrations present on the hump and on the dorsal and ventro-lateral surfaces of the hindbody lie in the same plane as the secondary gill lamellae and may provide anchorage against displacement forces. Elsewhere the tegument is highly folded forming a reticulum of lamellae and microvilli. The surface syncytium of the tegument in the region of the serrations possesses fibrous electron-dense bars, and a continuous fibrous electron-dense terminal web is present beneath the apical plasma membrane in all regions. The haptor consists of two asymmetrical rows of pincer-type clamps and a terminal lappet with a pair of hooks. Each clamp may be withdrawn into a cushion-like pad. Uniciliated sensory structures are found around the mouth and on the body surface, whereas non-ciliated papillae-like structures are present on the haptor and hindbody. A pair of cone-like sensilla is present on the lappet.  相似文献   

14.
Gerasev PI 《Parazitologiia》2001,35(6):545-551
The haptors Dactylogyrus spp., Anacanthorus sp., Trianchoratus sp. and Schilbetrematoides pseudodactylogyrus are investigated. On the base of the morphology, transfer of the domus, etc. a homology of the hooks in dactylogyrids (s. s.) and the pin-like structures (4 "A") in the haptor of Anacanthorinae and Dactylogyridae sensu Bychowsky et Nagibina, 1978 is demonstrated. The vestiges of the anchors in the haptor of dactylogyrids (s. l.), according to morphological data, correspond to the point of anchor formed during the ontogenesis. In S. pseudodactylogyrus the pins are redescribed as typical vestiges of the anchors.  相似文献   

15.
Thysanotohaptor n. gen. (Neocalceostomatidae) is proposed to accommodate Thysanotohaptor rex n. sp. collected from the gills of the blackfin sea catfish Arius jella Day (Siluriformes: Ariidae) from off the coast of Visakhapatnam, Bay of Bengal, Andhra Pradesh, India. Thysanotohaptor is differentiated from the other known neocalceostomatid genera by its species having multiple postgermarial testes (single testis in species of Neocalceostoma and Neocalceostomoides ), lacking a transverse bar associated with the ventral anchor pair (present in species of Neocalceostoma ), and possessing a disc-shaped haptor with a pleated marginal frill (frill absent in Neocalceostomoides spp.; Neocalceostoma spp. with delicate marginal membranes). The Neocalceostomatidae is considered valid within the Order Dactylogyridea based on its members having a haptor armed with 10 marginal and 4 ventral hooks and a germarium having a distal loop prior to uniting with the ootype; the family is not assigned to a suborder of Dactylogyridea because of uncertainty in part about the way in which the distribution of haptoral hooks evolved within the taxon.  相似文献   

16.
Sundatrema langkawiense n. g., n. sp. (Monogenea: Ancyrocephalidae) is described from the gills of the orbfish Ephippus orbis (Bloch) (Ephippidae) off the Island of Langkawi, Malaysia, in the Andaman Sea. This new genus has the ancyrocephalid characteristics of four anchors, 14 marginal hooks and two bars, but differs from other four-anchored monogenean genera, and notably from Parancylodiscoides Caballero & Bravo Hollis, 1961 (found on the ephippids Chaetodipterus spp. off Central and South America), by having a unique combination of features. These include a muscular genital sucker and a vas deferens and vagina on the same (sinistral) side of the body. It is similar to Parancylodiscoides in having four haptoral reservoirs opening at the anchoral apertures, four anchors, similar connecting bars and small marginal hooks. The new species is characterised by the above generic features and by possessing a small, short copulatory organ lacking an accessory piece. Diplectanum longiphallus MacCallum, 1915 (previously attributed to Ancyrocephalus Creplin, 1839, Tetrancistrum Goto & Kikuchi, 1917 and Pseudohaliotrema Yamaguti, 1953) is transferred to Parancylodiscoides as P. longiphallus (MacCallum, 1915) n. comb.  相似文献   

17.
Two new species of Monogenoidea were found parasitizing the cephalic lateral line canals of Percichthys trucha (Valenciennes) (Perciformes: Percichthyidae). These species are described as members of a newly proposed genus of Dactylogyridae. Cryptocephalum n. gen. is characterized by the site of infection and the combination of the several features: ventral and dorsal anchor/bar complexes, anchors with strongly elongated shaft and recurved point, shaft and point of dorsal anchors protruding laterally from haptor, hooks with 2 subunits and with pair 5 smaller than the others; gonads overlapping; coiled male copulatory organ with counterclockwise rings, accessory piece formed by 2 distinct parts, and a tubular, sclerotized ventral vagina. C ryptocephalum petreum n. sp. is characterized by having both anchor pairs protruding laterally from haptor, male copulatory organ with a coil of 2-1/2 rings, accessory piece tweezers-shaped, and sclerotized vaginal vestibule. Cryptocephalum spiralis n. sp. has ventral anchors protruding ventrally and dorsal ones protruding laterally, male copulatory organ with a coil of 1-1/2 rings, the antero-dorsal part of the accessory piece saddle-shaped, vaginal vestibule not present, and coiled vagina. This is the first record of Dactylogyridae species parasitizing the cephalic lateral line of fishes.  相似文献   

18.
Four new and one unidentified species of Neohaliotrema Yamaguti, 1965 were obtained from the gills of the Indo-Pacific sergeant Abudefduf vaigensis (Quoy & Gaimard) off Pulau Langkawi, Malaysia. The five species, N. malayense n. sp., N. bombini n. sp., N. andamanense n. sp., N. parvum n. sp. and an unidentified Neohaliotrema sp. (similar to N. macracanthum Zhukov, 1976), are described and distinguished based mainly on features of the haptor. Species of this genus are divisible into two groups, the ‘maomao group’, with two pairs of morphometrically modified ‘marginal’ hooks and a fenestrated haptor, and the ‘gracile group’, with morphologically similar marginal hooks and an entire haptor. With the exception of N. bombini n. sp., the species described fit within the ‘maomao group’. It is suggested that the more complex Neohaliotrema species of the ‘maomao group’ have modified hooks 1 and 2 on a haptoral ‘isthmus’ between two large apertures, i.e. ‘windows’, whereas the less complex species lacking these features are those of the ‘gracile group’. Neohaliotrema spp. have only a single pair of pigmented eye-spots. A fenestrated haptor is unique to the Neohaliotrema spp. of the ‘maomao group’. The generic diagnosis of Neohaliotrema is amended to include new data and a key to its known species is presented.  相似文献   

19.

Background

Monogeneans are flatworms (Platyhelminthes) that are primarily found on gills and skin of fishes. Monogenean parasites have attachment appendages at their haptoral regions that help them to move about the body surface and feed on skin and gill debris. Haptoral attachment organs consist of sclerotized hard parts such as hooks, anchors and marginal hooks. Monogenean species are differentiated based on their haptoral bars, anchors, marginal hooks, reproductive parts’ (male and female copulatory organs) morphological characters and soft anatomical parts. The complex structure of these diagnostic organs and also their overlapping in microscopic digital images are impediments for developing fully automated identification system for monogeneans (LNCS 7666:256-263, 2012), (ISDA; 457–462, 2011), (J Zoolog Syst Evol Res 52(2): 95–99. 2013;). In this study images of hard parts of the haptoral organs such as bars and anchors are used to develop a fully automated identification technique for monogenean species identification by implementing image processing techniques and machine learning methods.

Result

Images of four monogenean species namely Sinodiplectanotrema malayanus, Trianchoratus pahangensis, Metahaliotrema mizellei and Metahaliotrema sp. (undescribed) were used to develop an automated technique for identification. K-nearest neighbour (KNN) was applied to classify the monogenean specimens based on the extracted features. 50% of the dataset was used for training and the other 50% was used as testing for system evaluation. Our approach demonstrated overall classification accuracy of 90%. In this study Leave One Out (LOO) cross validation is used for validation of our system and the accuracy is 91.25%.

Conclusions

The methods presented in this study facilitate fast and accurate fully automated classification of monogeneans at the species level. In future studies more classes will be included in the model, the time to capture the monogenean images will be reduced and improvements in extraction and selection of features will be implemented.
  相似文献   

20.
Seasonal variations in size and shape of the marginal hooks, the anchors and the ventral bar of the opisthaptor of Gyrodactylus salaris Malmberg, 1957 were studied. The G. salaris specimens were collected from parr of Atlantic salmon Salmo salar L. in the River Batnfjordselva, north-western Norway. Samples were taken at roughly monthly intervals during a two-year period. The marginal hooks, the anchors and the ventral bar showed considerable seasonal variation in size, but varied only slightly in shape. The variation in 12 of the 14 characters measured showed a significant regression to the variation in the water temperature. The total length of the marginal hooks of G. salaris can be considerably longer than the previously reported maximum of 40 m for the species.  相似文献   

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